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Clinical Trials in Egypt / NCT07164638
Enrolling by invitation Not applicable

Lung Ultrasound Versus Inferior Vena Cava Collapsibility Index for Early Prediction of Volume Overload During Transurethral Resection of Prostate

NCT07164638 · tracked via the Priya Life Science Egypt tracker
Sponsor
Tanta University
Phase
Not applicable
Started
2024-10-30
Last updated
2025-09-10

Condition(s) studied

Lung Ultrasound ScoreTransurethral Resection (TUR) SyndromeProstate

Investigational drug(s) / intervention(s)

lung ultrasound (LUS)IVC collapsibility index

lung ultrasound (LUS): Serial lung ultrasound will be performed to patients enrolled in this study before the beginning of the surgery, every 15 minutes in the first 30 minutes, and then every 30 minutes for the rest of the operation.lung ultrasound will be used as a tool for monitoring of EVLW to identify early the subclinical pulmonary edema and ensure timely and correct diagnosis and appropriate management.

IVC collapsibility index: Serial assessment of IVC collapsibility will be used as a monitoring of volume overload in patients enrolled in this study. Basal IVC scanning using ultrasound will be performed before the start of the operation and serial IVC scanning will be done during the procedure every 15 minutes in the first 30 minutes, and then every 30 minutes for the rest of the operation.

Study summary

The aim of this study is to compare between accuracy of lung US and IVC CI for early prediction of volume overload during TURP.

Primary outcome:

The incidence of volume overload during transurethral resection of prostate.

Eligibility

Sex
MALE
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Male patient * American Society of Anesthesiologists classification II-III * scheduled for Transurethral resection of the prostate syndrome under spinal anesthesia. Exclusion Criteria: * Patient refusal. * Uncooperative patients. * Patients with major respiratory, cardiac, renal or hepatic disorders. * Patients whose ultrasound did not clearly show the inferior vena cava as (morbidly obese patients or patients with moderate to marked ascites). * Patients who have contraindications to spinal anesthesia (neurological disease, severe hypotension, coagulopathy, low fixed cardiac output).

Primary outcome measure(s)

  • incidence of volume overload — 2 HOURS

Trial sites (1)

FacilityCityRegionStatus
Tanta University Tanta Egypt

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07164638 on ClinicalTrials.gov ↗ ← All trials in Egypt